Sustained-release dexamfetamine in the treatment of chronic cocaine-dependent patients on heroin-assisted treatment: a randomised, double-blind, placebo-controlled trial

被引:55
作者
Nuijten, Mascha [1 ]
Blanken, Peter [1 ]
van de Wetering, Ben [2 ]
Nuijen, Bastiaan [3 ]
van den Brink, Wim [4 ]
Hendriks, Vincent M. [1 ,5 ]
机构
[1] Parnassia Addict Res Ctr PARC, Brijder Addict Treatment, Monsterseweg 83, NL-2553 RJ The Hague, Netherlands
[2] Antes Grp, Rotterdam, Netherlands
[3] Antoni van Leeuwenhoek Netherlands Canc Inst, Med Ctr Slotervaart, Amsterdam, Netherlands
[4] Univ Amsterdam, Acad Med Ctr, Ctr Psychiat, Amsterdam Inst Addict Res, Tafelbergweg 25, NL-1105 BC Amsterdam, Netherlands
[5] Leiden Univ, Dept Child & Adolescent Psychiat, Med Ctr, Curium, Leiden, Netherlands
关键词
USE DISORDERS; AGONIST-LIKE; PHARMACOTHERAPY; PRESCRIPTION; MEDICATION; ADHERENCE; EFFICACY; ADDICTS; ALCOHOL;
D O I
10.1016/S0140-6736(16)00205-1
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Heroin-assisted treatment is effective for methadone treatment-refractory heroin-dependent patients, but continued comorbid cocaine dependence remains problematic. Sustained-release dexamfetamine is a promising agonist pharmacotherapy for cocaine dependence and we aimed to assess its acceptance, efficacy, and safety. Methods In this multicentre, randomised, double-blind, placebo-controlled trial, patients who were treatment-refractory, as indicated by at least two earlier failed treatments aimed at reducing or abstaining from cocaine use, and who regularly (>= 8 days/month) used crack-cocaine were enrolled from four heroin-assisted treatment centres in the Netherlands. Eligible patients were randomly assigned (1: 1) to receive either 12 weeks of daily, supervised prescription of 60 mg/day oral sustained-release dexamfetamine or placebo in addition to co-prescribed methadone and diacetylmorphine. Randomisation was done by the collaborating pharmacist, using a computer-generated random number sequence with stratification by treatment centre in blocks of four per stratum. Randomisation was masked to patients, staff, and researchers throughout the study. The primary outcome was the number of self-reported days of cocaine use during study treatment, assessed every 4 weeks. Primary and safety analyses were done in the intention-to-treat population. The study was registered with the European Union Drug Regulating Authorities Clinical Trials (EUdraCT 2013-004024-11) and with The Netherlands Trial Register (NTR2576). Findings Between Aug 8, 2014, and Feb 27, 2015, 111 patients were assessed for eligibility, of whom 73 were enrolled and randomised; 38 patients were assigned to the sustained-release dexamfetamine group and 35 to the placebo group. Sustained-release dexamfetamine treatment resulted in significantly fewer days of cocaine use than placebo treatment (mean 44.9 days [SD 29.4] vs 60.6 days [24.3], respectively [95% CI of difference 3.1-28.4]; p=0.031; Cohen's standardised effect size d=0.58). One or more adverse events were reported by 28 (74%) patients in the dexamfetamine group and by 16 (46%) patients in the placebo group. Most adverse events were transient and well-tolerated. Interpretation Sustained-release dexamfetamine is a well accepted, effective, and safe agonist pharmacotherapy for comorbid treatment-refractory cocaine dependence in heroin-dependent patients in heroin-assisted treatment. Future research should aim to replicate these findings in chronic cocaine-dependent and other stimulant-dependent patients in more routine treatment settings, including strategies to optimise treatment adherence like medication management interventions and contingency management.
引用
收藏
页码:2226 / 2234
页数:9
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